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Ultrasound reveals diaphragm changes in sleep apnea patients

NCT ID NCT07370376

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how well the diaphragm works in people with obstructive sleep apnea (OSA). Researchers used ultrasound to measure diaphragm movement in 60 adults with OSA. The goal was to see if diaphragm function is linked to how severe the sleep apnea is.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

60 people

The number who actually took part.

Started

Mar 2023

Finished

Mar 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patients visiting the Sleep Disordered Breathing (SDB) Unit at the Chest Medicine Department and diagnosed with obstructive sleep apnea (OSA) were included if they met the following criteria: Age 18-65 years.; OSA group: Newly diagnosed OSA confirmed by full-night polysomnography (PSG) with apnea-hypopnea index (AHI) \> 5 events/hour; Control group: Patients with AHI \< 5 events/hour on PSG; Willingness to participate in the study.

Ages

18 years and older

Sex

Anyone

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients visiting the Sleep Disordered Breathing (SDB) Unit at the Chest Medicine Department and diagnosed with obstructive sleep apnea (OSA) were included if they met the following criteria: * Age 18-65 years. * Willingness to participate in the study. Exclusion Criteria: * Patients were excluded if they had any of the following conditions: * Refusal to participate in the study * Age \<18 or \>65 years * Systemic organ failure, including heart failure, stroke, renal failure, or liver failure; Uncontrolled diabetes mellitus * Diagnosed obesity hypoventilation syndrome (OHS) or other sleep disorders apart from OSA * Chronic respiratory diseases such as COPD, bronchial asthma, or restrictive lung disease * OSA patients already receiving therapy (CPAP, oral appliances, or upper airway surgery) * Neuromuscular disorders or other conditions affecting diaphragmatic function (malnutrition, chest trauma, or immobility) * Use of steroids or uncontrolled autoimmune diseases.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Mohamed AbdElmoniem

    Al Mansurah, 35516, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.